GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Gene Symbol

Gene ID

Organism

Source

Display
results per page.

Clear

Submissions

GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **1301 - 1325** of **15957** in total

« First

‹ Prev

…

49

50

51

52

53

54

55

56

57

…

Next ›

Last »
Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:0050814	temtamy preaxial brachydactyly syndrome Aliases: PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE	chsy1.L chsy1.S	108711484 108712816	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0111238	congenital muscular dystrophy-dystroglycanopathy type A13 Aliases: MDDGA13 Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13	b4gat1.L	108713949	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0110658	congenital myasthenic syndrome 15 Aliases: CMS15 congenital myasthenic syndrome 15 without tubular aggregates	alg14.L alg14.S	108714370 108715652	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0110567	autosomal dominant nonsyndromic deafness 41 Aliases: DFNA41 autosomal dominant deafness 41	p2rx2.L	108715297	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:2565	macular corneal dystrophy Aliases: Fehr corneal dystrophy MACULAR DYSTROPHY, CORNEAL, 1	chst6.L chst6.S	108715440 444431	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0081180	autosomal recessive intellectual developmental disorder 12	LOC108715547	108715547	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0080414	developmental and epileptic encephalopathy 15 Aliases: DEE15 early infantile epileptic encephalopathy 15	LOC108715547	108715547	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:10584	retinitis pigmentosa Aliases: pericentral pigmentary retinopathy	pomgnt1.L pomgnt1.S prph2.S rho.L rho.S	108715858 380209 398002 414570 495292	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:11105	fundus albipunctatus Aliases: Pigmentary retinal dystrophy retinitis punctata albescens	prph2.S rho.L rho.S	108715858 380209 398002	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0110862	congenital stationary night blindness autosomal dominant 1 Aliases: CSNBAD1 rhodopsin-related congenital stationary night blindness	rho.L rho.S	108715858 380209	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:8499	night blindness Aliases: nyctalopia	rho.L rho.S	108715858 380209	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0110372	retinitis pigmentosa 4 Aliases: RP4	rho.L rho.S	108715858 380209	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:9206	Barrett's esophagus Aliases: Barrett esophagus Barrett's esophagus with esophagitis Barrett's oesophagus Barrett's ulcer of esophagus Barretts syndrome ulcerative esophagitis	b3gat2.L b3gat2.S bmp4.S	108716933 399322 733177	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0090075	hypogonadotropic hypogonadism 15 with or without anosmia	hs6st1.L hs6st1.S	108717161 373566	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0080693	Noonan syndrome-like disorder with loose anagen hair 2	ppp1cb.L ppp1cb.S	108717671 443852	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0080081	nonsyndromic congenital nail disorder 3	plcd1.L plcd1.S	108718712 108719811	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0040094	autoimmune glomerulonephritis	FGL2	10875	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080301	atypical hemolytic-uremic syndrome	ADAMTS13 C3 CD46 CFB CFH CFHR1 CFHR3 CFI THBD	10878 11093 3075 3078 3426 4179 629 7056 718	Homo sapiens (human)	Alliance of Genome Resources
DOID:3498	pancreatic ductal adenocarcinoma Aliases: ductal adenocarcinoma of the pancreas	AKR7A2 CALR CD59 CFHR3 E2F1 EIF5A EIF5AL1 FOXM1 FUBP1 GOT1 HSPA8 JAK1 PIK3CG PLD1 PTPRB PTPRM RAC1 RALA TGFB1 TGFB2 TGFB3 TGFBR1 VEGFD VNN1	10878 143244 1869 1984 2277 2305 2805 3312 3716 5294 5337 5787 5797 5879 5898 7040 7042 7043 7046 811 8574 8876 8880 966	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110014	age related macular degeneration 1 Aliases: ARMD1 age related maculopathy 1	APOE CFHR1 CFHR3 HMCN1 VLDLR	10878 3078 348 7436 83872	Homo sapiens (human)	Alliance of Genome Resources
DOID:3969	thyroid gland papillary carcinoma Aliases: Papillary carcinoma of the Thyroid gland	ATM BRD4 CAT CDH1 CTNNB1 HABP2 HRAS KMT2D LEF1 MINPP1 MYC NKX2-1 NRAS PLAU RUNX3 SRGAP1 TP53 WDR3 XRCC1	10885 1499 23476 3026 3265 4609 472 4893 51176 5328 57522 7080 7157 7515 8085 847 864 9562 999	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050560	Walker-Warburg syndrome Aliases: HARD syndrome cerebroocular dysplasia-muscular dystrophy syndrome	B4gat1 Col4a1 Crppa Fkrp Fktn Pomgnt1 Pomt1 Pomt2 Rxylt1	108902 12826 216395 217734 243853 246179 68273 75847 99011	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050588	muscular dystrophy-dystroglycanopathy type B1 Aliases: CMD due to dystroglycanopathy Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1	B4gat1 Dag1 Fkrp Fktn Large1 Pomgnt1 Pomt1	108902 13138 16795 243853 246179 68273 99011	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0111238	congenital muscular dystrophy-dystroglycanopathy type A13 Aliases: MDDGA13 Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13	B4gat1	108902	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1909	melanoma Aliases: Naevocarcinoma malignant melanoma	AGER ASS1 ATRX BMP4 BRCA2 BRD2 BRD4 CAT CD40 CHI3L1 CTLA4 EHMT2 ELN ERCC5 ESR1 FAS FASLG FLT1 GALC GGT1 GPER1 HLA-DQA1 ICAM1 IL1RN ING3 JUNB KDM2A KDR KIT LRP1B LTA MC1R MGMT MITF NFKB1 NRAS NUF2 PPARGC1A RHOB RNASET2 SETDB1 SOD2 SOX2 SPP1 TERT TLR4 TP53 TYR VEGFA	10891 10919 1116 1493 177 2006 2073 2099 22992 2321 23476 2581 2678 2852 3117 3383 355 3557 356 3726 3791 3815 388 4049 4157 4255 4286 445 4790 4893 53353 54556 546 6046 652 6648 6657 6696 675 7015 7099 7157 7299 7422 83540 847 8635 958 9869	Homo sapiens (human)	Alliance of Genome Resources

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements